Hello ladies, my stepson is almost 11 and lives full time with me and his dad and was diagnosed with adhd at age 6, he also was horrendous, running every where, throwing things, attacking staff and other children at school, unable to follow instructions, unable to sit still etc etc. After diagnosis he was prescribed a form of ritalin once a day in the moring, great, till it wore off so they introduced a 2nd dose at lunchtime but of course the school won't administter it so i used to have to go in, then he was put on Concerta which is the slow release version and that was so much better.
After 3 years the dose was upped from 18mg to 36mg as both the school and us noticed a gradual change in his behaviour so the tried the higher dose and so far it seems to be going well. On the days when for whatever reason he hasn't had his tablet we notice fairly quickly, he is unable to sit still, hands constantly moving, twitching fingers and toes etc . The only detention he has ever had at school was the day he'd had no tablet. Sorry should have said that at aged 7 he was moved to a special school, at first we didn't want him to go there but it's the best thing we could have done for him, he is now making progress in leaps and bounds academically, behaviourally he is so improved and ignores other children disruping the class where as 2 years ago he would have joined in, he is polite, well mannered and a joy to have around, very different from the tasmanian devil who came to live with us 5years ago! The school are even planning on moving him to mainstream high school in sept so he joins with his peers, they will keep his place at special school until they are confident about his integration at the mainstream school.
The consultants etc are usually reluctant to diagnose adhd before age 7, however even though your son is only 5 he is entitled to help at school, ask to speak to the SEN there to see if any support can be arranged for him to try and include him in school, if you can prevent him from being excluded or only attending part time it's better in the long run.
There are side effects for the drugs and they don't work for everyone but it is worth a try.
I wish i had found something like this forum when they first came to live with us as i was also at the end of my tether with them and was so glad to have the support of the school and doctors etc in helping me manage his behaviour (had no children or experience of them at all then!!) and they were fantastic, even now i still rely on one of the ta's from school for advice and support, but now i work with her as a ta for children with special needs!
If i can be of any help or support to anyone please just ask
Helen